Canonical Allele Identifier: PA2825948210
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407899
ClinVar RCV Id: RCV001909377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Gly1812Arg
CA392222554
NM_001160227.2:c.5434G>C
CA392222555
NM_001160227.2:c.5434G>A